Vector Database
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Vector database is a digital-only collection of vector backbone information compiled by Addgene from third party sources.
This vector is NOT available from Addgene and the database is no longer actively maintained.
This vector is not available from Addgene.
Plasmid: pJLS1022
Information
- Plasmid Type
- Unspecified
- Cloning Method
- Unknown
- Notes
- To produce pJLS1022, the pJLS1021 (#M10299) BamHI site was treated with nuclease S1. The region controlling translation of the cat gene has been varied structurally so that the gene is under control of the lac promoter. Altering the potential for secondary structure formation within the translation control region causes a ten-fold variation in the synthesis of the CAT enzyme, whereas varying the distance between the ribosome binding site and the start codon from 7 to 13 bases does not significantly affect the yield of CAT enzyme. If the Shine Dalgarno sequence is situated in a region of mRNA capable of base pairing, the efficiency of translation is decreased. The start codon can initiate translation efficiently even when located in a segment capable of duplex formation. If translation is initiated upstream of the cat start codon, then out of frame overlapping translation reduces CAT production by 90% and in frame overlapping translation prevents detectable initiation of protein synthesis at the cat gene start codon and yields only fusion proteins. NCBI gi: 208715 Hosts: E.coli. Related vectors: pJLS1021. (Information source: VectorDB ( http://seq.yeastgenome.org/vectordb ).)
- GenBank
- M10301
- Stable
- Unspecified
- Constitutive
- Unspecified
- Viral/Non-Viral
- Unspecified